csf pleocytosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased white blood cell count in the cerebrospinal fluid. (Human Phenotype Ontology, HP_0012229)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012229
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Genes

4 genes associated with the csf pleocytosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PRF1 perforin 1 (pore forming protein)
RNASEH2A ribonuclease H2, subunit A
RNASEH2B ribonuclease H2, subunit B
TREX1 three prime repair exonuclease 1